US4252714A - Flame resistant resin compositions - Google Patents
Flame resistant resin compositions Download PDFInfo
- Publication number
- US4252714A US4252714A US05/859,838 US85983877A US4252714A US 4252714 A US4252714 A US 4252714A US 85983877 A US85983877 A US 85983877A US 4252714 A US4252714 A US 4252714A
- Authority
- US
- United States
- Prior art keywords
- styrene
- parts per
- per hundred
- unsaturated polyester
- diallyl maleate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000011342 resin composition Substances 0.000 title description 2
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 claims abstract description 16
- 229920006337 unsaturated polyester resin Polymers 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 7
- UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 abstract description 14
- -1 alkyl phosphates Chemical class 0.000 abstract description 14
- 235000021317 phosphate Nutrition 0.000 abstract description 14
- 239000003999 initiator Substances 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 12
- 229910052698 phosphorus Inorganic materials 0.000 description 12
- 239000011574 phosphorus Substances 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
- 239000001301 oxygen Substances 0.000 description 10
- 229910052760 oxygen Inorganic materials 0.000 description 10
- 239000003063 flame retardant Substances 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 9
- 239000010452 phosphate Substances 0.000 description 8
- 229920006305 unsaturated polyester Polymers 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical group CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229910000410 antimony oxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 2
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 2
- HGTUJZTUQFXBIH-UHFFFAOYSA-N (2,3-dimethyl-3-phenylbutan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(C)(C)C(C)(C)C1=CC=CC=C1 HGTUJZTUQFXBIH-UHFFFAOYSA-N 0.000 description 1
- LABRPRANVKSMGP-UHFFFAOYSA-N 1,3,2-dioxaphosphinane Chemical group C1COPOC1 LABRPRANVKSMGP-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- YAFOVCNAQTZDQB-UHFFFAOYSA-N octyl diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(OCCCCCCCC)OC1=CC=CC=C1 YAFOVCNAQTZDQB-UHFFFAOYSA-N 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
Definitions
- the present invention pertains to flame resistant styrene-unsaturated polyester resin systems and to a method of decreasing the flammability of such styrene-unsaturated polyester resins. More particularly, this invention is directed to styrene-unsaturated polyester resin compositions prepared by reacting a mixture of styrene-polyester resins with diallyl maleate and an alkyl phosphate.
- Organic substances containing phosphorus are well known as flame retardants for synthetic plastics, elastomers, fibers, films, etc., as well as for many naturally occurring combustible substances.
- the effectiveness of organic phosphorus flame retardants varies widely depending on the base substance but, in general, organic phosphorus is not known as a highly active flame retardant element for most synthetic resin systems. Frequently, the amount needed to achieve a high level of flame resistance is excessive and the resin matrix is unable to accommodate the high loading, that is, the resin and high level of organic phosphorus compounds are incompatible and, in addition, all useful mechanical properties are lost through modification with the flame retardant.
- Enhancement of flame retardant activity by combinations of materials is not necessarily limited to cases in which both components exercise activity individually.
- certain aromatic hydrocarbons of the type 2,3-dimethyl-2,3-diphenyl-butane and polymeric isopropylarylenes, respectively are disclosed as strong activators for organic bromine in flame retardant polystyrene compositions.
- Phosphoric acid esters have been used as solvents for flameproofing agents such as pentachlorophenol. The application of such solutions to cellulosic products is described in U.S. Pat. No. 2,926,096.
- U.S. Pat. No. 3,511,857 discloses flame resistant polyester compositions prepared by reacting a polybasic acid or anhydride with the free hydroxyl groups in the 1,3,2-dioxaphosphorinane ring of phosphonic acid.
- phosphate esters containing at least one alkyl ester group are rendered much more effective as flame retardants for styrene crosslinked polyesters when used in conjunction with diallyl maleate. It is noteworthy that diallyl maleate in the absence of alkyl phosphate causes only a slight elevation of the Oxygen Index amounting to approximately one unit per ten parts of diallyl maleate added to a hundred of resin.
- alkyl phosphates are so affected although a mixed alkylaryl phosphate (octyl diphenyl phosphate) gives similar results as do alkyl phosphate having the formula ##STR1## wherein R 1 is selected from the group consisting of hydrogen radicals and alkyl radicals, and R 2 and R 3 are selected from the group consisting of alkyl radicals and aryl radicals.
- the flame resistance of the styrene crosslinked resin composition will vary with the structure of the alkyl phosphate. If a high level of flame resistance is desired (an Oxygen Index of 26 or higher), it is necessary that sufficient alkyl phosphate be added to the styrene-unsaturated polyester to supply an effective amount, from about 0.5 weight percent to as much as about 5 weight percent of elemental phosphorus (P) based on the weight of styrene-unsaturated polyester.
- P elemental phosphorus
- diallyl maleate should be added to the styrene-unsaturated polyester in amounts of about 10 to about 40 parts per hundred.
- the ratio of diallyl maleate to phosphorus (P) in the styrene-unsaturated polyester system may vary within the range of from about 2:1 to about 50:1. Particularly preferred is a styrene-unsaturated polyester system containing from about 0.6 to 1.8 weight percent triethyl phosphate and a weight ratio of diallyl maleate to elemental phosphorus in the range of from about 10:1 to 50:1.
- the weight percent phosphorus is desirably about 0.8 weight percent and the ratio of diallyl maleate to phosphorus is about 37:1.
- the invention is further illustrated by the following examples in which all quantities are given in parts by weight.
- the Oxygen Index reported in the examples and tables is determined by test method D2863-76.
- a styrene-unsaturated polyester system is prepared by dissolving a 1:1 maleic-isophthalic acid ester of dipropylene glycol (manufactured and sold by the Diamond Chemical Co. under the trade name DIONE ISO 6421) in an equal weight of styrene to form a 50% solution.
- DIONE ISO 6421 dipropylene glycol
- the cured specimens are relatively easily removed from the glass tubes by chilling in ice which, coupled with the contraction during curing, resulted in sufficient shrinkage to cause separation of a solid resin from the glass walls. Oxygen Index measurements are then made on the rod specimens.
- Table I lists the results obtained from combinations of diallyl maleate with various phosphate esters. Of the phosphates employed, triethyl phosphate is most effective.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Diallyl maleate in combination with alkyl phosphates, including mixed alkyl aryl phosphates, when added to styrene-unsaturated polyester resin systems and cured with a free-radical forming initiator provides a high level of flame resistance.
Description
The present invention pertains to flame resistant styrene-unsaturated polyester resin systems and to a method of decreasing the flammability of such styrene-unsaturated polyester resins. More particularly, this invention is directed to styrene-unsaturated polyester resin compositions prepared by reacting a mixture of styrene-polyester resins with diallyl maleate and an alkyl phosphate.
Organic substances containing phosphorus are well known as flame retardants for synthetic plastics, elastomers, fibers, films, etc., as well as for many naturally occurring combustible substances. The effectiveness of organic phosphorus flame retardants varies widely depending on the base substance but, in general, organic phosphorus is not known as a highly active flame retardant element for most synthetic resin systems. Frequently, the amount needed to achieve a high level of flame resistance is excessive and the resin matrix is unable to accommodate the high loading, that is, the resin and high level of organic phosphorus compounds are incompatible and, in addition, all useful mechanical properties are lost through modification with the flame retardant.
Where resin modifiers are of limited effectiveness, it is well known in the art to seek synergists involving combinations of agents to permit the modifiers to be employed at total concentrations which are less than for the individual agents acting alone. Although few synergistic combinations have been definitely established among flame retardants, one couple, namely, the antimony-halogen combinations, is so widely employed that synergism is universally accepted even though there is no general agreement as to mechanism. A similar synergism has recently been reported for molybdenum oxide and ammonium molybdate in combination with halogen. (D. A. Church and F. W. Moore, Plastics Engineering 31, No. 12, December 1975.) Further, molybdenum oxide combined with antimony oxide reportedly exhibits a synergism vs. the individual oxides when all are compared in chlorine containing systems.
Synergistic effects with phosphorus are not as readily evident as with the above metal oxides. Phosphorus plus chlorine generally yields barely additive effects. However, it is becoming recognized that phosphorus plus bromine produces synergistic effects in a number of systems.
Enhancement of flame retardant activity by combinations of materials is not necessarily limited to cases in which both components exercise activity individually. For example, in patents to Badische Anilin and Soda-Fabrik Aktiengesellschaft (U.S. Pat. Nos. 3,420,786 and 3,457,204) certain aromatic hydrocarbons of the type 2,3-dimethyl-2,3-diphenyl-butane and polymeric isopropylarylenes, respectively, are disclosed as strong activators for organic bromine in flame retardant polystyrene compositions.
Phosphoric acid esters have been used as solvents for flameproofing agents such as pentachlorophenol. The application of such solutions to cellulosic products is described in U.S. Pat. No. 2,926,096.
The fire resistant properties of epoxyalkyl esters of phosphoric acid are taught in U.S. Pat. No. 3,056,806.
U.S. Pat. No. 3,511,857 discloses flame resistant polyester compositions prepared by reacting a polybasic acid or anhydride with the free hydroxyl groups in the 1,3,2-dioxaphosphorinane ring of phosphonic acid.
Both alkyl and aryl phosphates provide a modest level of flame retardance to styrene crosslinked polyester systems. Oxygen Index increases at a rate of about 1.5 units per percent phosphorus present in the complete formulation. Thus, use of organic phosphates as flame retardants as the sole active constituent has been very limited since relatively large quantities are required to attain even a modest level of flame resistance. Such styrene-containing systems normally employ chlorine or, more recently, bromine-containing polyesters which, when synergized with antimony oxide, can provide a very high level of flame resistance.
In accordance with the present invention, it has now been discovered that phosphate esters containing at least one alkyl ester group are rendered much more effective as flame retardants for styrene crosslinked polyesters when used in conjunction with diallyl maleate. It is noteworthy that diallyl maleate in the absence of alkyl phosphate causes only a slight elevation of the Oxygen Index amounting to approximately one unit per ten parts of diallyl maleate added to a hundred of resin. Only alkyl phosphates are so affected although a mixed alkylaryl phosphate (octyl diphenyl phosphate) gives similar results as do alkyl phosphate having the formula ##STR1## wherein R1 is selected from the group consisting of hydrogen radicals and alkyl radicals, and R2 and R3 are selected from the group consisting of alkyl radicals and aryl radicals.
The flame resistance of the styrene crosslinked resin composition will vary with the structure of the alkyl phosphate. If a high level of flame resistance is desired (an Oxygen Index of 26 or higher), it is necessary that sufficient alkyl phosphate be added to the styrene-unsaturated polyester to supply an effective amount, from about 0.5 weight percent to as much as about 5 weight percent of elemental phosphorus (P) based on the weight of styrene-unsaturated polyester.
The diallyl maleate should be added to the styrene-unsaturated polyester in amounts of about 10 to about 40 parts per hundred.
The ratio of diallyl maleate to phosphorus (P) in the styrene-unsaturated polyester system may vary within the range of from about 2:1 to about 50:1. Particularly preferred is a styrene-unsaturated polyester system containing from about 0.6 to 1.8 weight percent triethyl phosphate and a weight ratio of diallyl maleate to elemental phosphorus in the range of from about 10:1 to 50:1. When the trialkyl phosphate is tributyl phosphate, the weight percent phosphorus is desirably about 0.8 weight percent and the ratio of diallyl maleate to phosphorus is about 37:1.
The invention is further illustrated by the following examples in which all quantities are given in parts by weight. The Oxygen Index reported in the examples and tables is determined by test method D2863-76.
A styrene-unsaturated polyester system is prepared by dissolving a 1:1 maleic-isophthalic acid ester of dipropylene glycol (manufactured and sold by the Diamond Chemical Co. under the trade name DIONE ISO 6421) in an equal weight of styrene to form a 50% solution. To 100 parts of this styrene-unsaturated polyester solution is added diallyl maleate and tributyl phosphate in the amounts indicated in Table I, and 3 parts per hundred of benzoyl peroxide. Each solution is agitated until homogeneous, then deaerated and sealed in quarter inch by eight inch glass tubes for curing. Determinations of curing characteristics by Differential Scanning Calorimetry indicate reaction initiation for this initiator-resin combination occurs in the range of 70° to 75° C. Further, samples cured overnight in this temperature range show no residual energy, i.e., all chemical reactions capable of occurring had indeed occurred during this thermal exposure. All samples were, therefore, cured by placing the quarter inch specimens (in glass tubing) in a water bath maintained at 70° to 75° C. and heated a minimum of 16 hours.
The cured specimens are relatively easily removed from the glass tubes by chilling in ice which, coupled with the contraction during curing, resulted in sufficient shrinkage to cause separation of a solid resin from the glass walls. Oxygen Index measurements are then made on the rod specimens.
Table I lists the results obtained from combinations of diallyl maleate with various phosphate esters. Of the phosphates employed, triethyl phosphate is most effective.
TABLE I
______________________________________
a. Styrene-Polyester System Containing
Tributyl Phosphate-Diallyl Maleate Combinations
DAM TBP Oxygen
(phr).sup.1 (phr) P (%) Index
______________________________________
0 10 1.03 21.2
0 30 2.61 22.3
10 10 0.94 20.5
10 39 2.42 23.2
30 10 0.81 28.0
30 30 2.12 23.2
30 5 1.42 22.2
30 15 1.17 22.2
20 10 0.87 24.1
40 10 0.75 23.2
______________________________________
b. Styrene-Polyester Systems Containing
Triethyl Phosphate-Diallyl Maleate Combinations
DAM TEP Oxygen
(phr).sup.1 (phr) P (%) Index
______________________________________
0 0 0.0 19.0
10 0 0.0 19.9
40 0 0.0 22.2
0 10 1.50 23.0
0 40 4.71 23.3
10 10 1.38 24.9
10 40 4.40 24.9
40 10 1.10 32.4
40 40 3.67 23.2
40 5 0.56 25.2
40 15 1.60 20.2
30 0 0.0 23.2
30 5 0.61 30.4
30 10 1.18 26.0
30 15 1.71 20.5
20 5 0.66 20.5
20 10 1.27 20.5
20 15 1.84 28.0
20 20 2.36 26.0
______________________________________
c. Styrene-Polyester Systems Containing
Octyl Diphenyl Phosphate-Diallyl Maleate Combination
DAM Sanitizer Oxygen
(phr).sup.1
141 (phr) P (%) Index
______________________________________
0 10 0.76 20.5
30 5 0.31 21.2
30 10 0.59 21.2
30 15 0.86 21.0
40 5 0.29 20.2
40 10 0.55 28.0
40 15 0.81 26.0
______________________________________
d. Isopropyl Phenyl/Phenyl Phosphate - Diallyl
Maleate Combinations
DAM Triaryl Oxygen
(phr) Phosphate (phr)
P (%) Index
______________________________________
0 10 0.68 20.5
0 30 1.73 22.5
10 10 0.63 20.5
10 30 1.61 21.2
30 10 0.54 21.0
30 30 1.41 21.0
______________________________________
e. Styrene-Polyester Systems Containing
Combinations of Diethyl Phosphate [(EtO).sub.2 POOH]
With Diallyl Maleate
DAM DEP Oxygen
(phr).sup.1 (phr) P (%) Index
______________________________________
0 0 0 19.0
0 10 1.77 22.2
0 40 5.57 22.2
10 10 1.63 23.2
40 10 1.30 26.8
10 40 5.20 26.8
40 40 4.33 29.6
______________________________________
.sup.1(phr) = parts per hundred of styreneunsaturated polyester.
Claims (2)
1. A flame resistant styrene-unsaturated polyester resin composition comprising said styrene-unsaturated polyester resin in combination with at least 10 parts per hundred and no more than 40 parts per hundred of diallyl maleate and at least 10 parts per hundred but no more than 40 parts per hundred of diethyl phosphate; the total quantity of diallyl maleate and diethyl phosphate present in said styrene-unsaturated polyester resin being at least 50 and no more than 80 parts per hundred.
2. The method of improving the flame resistance of a styrene-unsaturated polyester resin which comprises adding to said styrene-unsaturated polyester resin, prior to polymerization from about 10 parts per hundred to about 40 parts per hundred of diallyl maleate and from about 10 parts per hundred to about 40 parts per hundred of diethyl phosphate, the total amount of diallyl maleate and diethyl phosphate added to said styrene-unsaturated polyester resin being no less than 50 and no more than 80 parts per hundred; and heating the mixture of polymerization temperature in the presence of a catalyst.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/859,838 US4252714A (en) | 1977-12-12 | 1977-12-12 | Flame resistant resin compositions |
| CA316,232A CA1105171A (en) | 1977-12-12 | 1978-11-14 | Flame resistant resin compositions |
| JP14733878A JPS5486592A (en) | 1977-12-12 | 1978-11-30 | Fireeresistant resin composition |
| ES475878A ES475878A1 (en) | 1977-12-12 | 1978-12-11 | Flame resistant resin compositions and method of preparing an unsaturated polyester resin with improved flame resistance. |
| IT30710/78A IT1192593B (en) | 1977-12-12 | 1978-12-11 | FLAME RESISTANT RESIN BASED COMPOSITION |
| EP78300795A EP0002601A1 (en) | 1977-12-12 | 1978-12-12 | Flame resistant resin compositions and method of preparing an unsaturated polyester resin with improved flame resistance |
| US06/016,581 US4207269A (en) | 1977-12-12 | 1979-03-01 | Flame resistant resin compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/859,838 US4252714A (en) | 1977-12-12 | 1977-12-12 | Flame resistant resin compositions |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/011,739 Division US4213889A (en) | 1979-02-13 | 1979-02-13 | Flame resistant resin compositions |
| US06/016,581 Continuation-In-Part US4207269A (en) | 1977-12-12 | 1979-03-01 | Flame resistant resin compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4252714A true US4252714A (en) | 1981-02-24 |
Family
ID=25331840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/859,838 Expired - Lifetime US4252714A (en) | 1977-12-12 | 1977-12-12 | Flame resistant resin compositions |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4252714A (en) |
| EP (1) | EP0002601A1 (en) |
| JP (1) | JPS5486592A (en) |
| CA (1) | CA1105171A (en) |
| ES (1) | ES475878A1 (en) |
| IT (1) | IT1192593B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7644889B2 (en) | 2006-07-18 | 2010-01-12 | Insitu, Inc. | Fluid sensing system and methods, including vehicle fuel sensors |
| JPWO2018131484A1 (en) * | 2017-01-10 | 2019-11-07 | 株式会社大阪ソーダ | Unsaturated polyester resin composition |
| JP2021105068A (en) * | 2018-03-30 | 2021-07-26 | 株式会社大阪ソーダ | Thermosetting resin composition |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2822340A (en) * | 1955-10-12 | 1958-02-04 | American Cyanamid Co | Flame resistant polyester resinous compositions containing combined halogens and phosphorous and certain alkaline earth metal salts and the process of preparing the same |
| US3758638A (en) * | 1971-10-26 | 1973-09-11 | Ppg Industries Inc | Unsaturated polyesters with reduced smoke levels |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3232893A (en) * | 1962-06-27 | 1966-02-01 | Reichhold Chemicals Inc | Foamed polyester-maleic anhydride compositions and method of making the same |
| US3873496A (en) * | 1973-06-11 | 1975-03-25 | Fmc Corp | Flame-retardant polyester compositions |
-
1977
- 1977-12-12 US US05/859,838 patent/US4252714A/en not_active Expired - Lifetime
-
1978
- 1978-11-14 CA CA316,232A patent/CA1105171A/en not_active Expired
- 1978-11-30 JP JP14733878A patent/JPS5486592A/en active Pending
- 1978-12-11 IT IT30710/78A patent/IT1192593B/en active
- 1978-12-11 ES ES475878A patent/ES475878A1/en not_active Expired
- 1978-12-12 EP EP78300795A patent/EP0002601A1/en not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2822340A (en) * | 1955-10-12 | 1958-02-04 | American Cyanamid Co | Flame resistant polyester resinous compositions containing combined halogens and phosphorous and certain alkaline earth metal salts and the process of preparing the same |
| US3758638A (en) * | 1971-10-26 | 1973-09-11 | Ppg Industries Inc | Unsaturated polyesters with reduced smoke levels |
Also Published As
| Publication number | Publication date |
|---|---|
| IT7830710A0 (en) | 1978-12-11 |
| JPS5486592A (en) | 1979-07-10 |
| EP0002601A1 (en) | 1979-06-27 |
| IT1192593B (en) | 1988-04-20 |
| ES475878A1 (en) | 1979-12-01 |
| CA1105171A (en) | 1981-07-14 |
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